FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HEYER-SCHULTE SYRINGO PERITONEAL SHUNT

K Number: K854049 · Decision Nov 27, 1985
Classifications
1
FEI Numbers
68
Registration Numbers
69
Same Product Code
257
Applicant Total
31
Review Days
55

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Basic Information

Device Name
HEYER-SCHULTE SYRINGO PERITONEAL SHUNT
K Number
K854049
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5550
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
American V. Mueller
Date Received
October 3, 1985
Decision Date
November 27, 1985
Product Code
JXG
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JXG Shunt, Central Nervous System And Components

Similar 510(k) Clearances

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Other Clearances by American V. Mueller

K Number Device Name
K873771 HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTRO
K873332 MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM
K871685 HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS
K864676 HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM
K862772 V. MUELLER (R) GOOSENECK CIRCULAR STAPLER
K861471 V. MUELLER VITAL CLIP-HEMOSTATIC CLIP
K854568 V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP
K851082 V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
K851974 V. MUELLER VITAL SKIN STAPLER
K850947 V-MUELLER INVERTED LINEAR ANASTOMOSIS INSTRUMENTS
Search all 31 clearances from American V. Mueller →